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15474-96-1

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15474-96-1 Usage

General Description

CHLOROACETYL-GLYCYL-GLYCINE is a chemical compound that is used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes. It is also known for its antimicrobial properties and is often used in the formulation of disinfectants and antiseptic products. CHLOROACETYL-GLYCYL-GLYCINE is a derivative of glycine, an essential amino acid, and contains a chlorine atom and an acetyl group attached to the glycine molecule. Its chemical structure allows it to act as a potent antimicrobial agent, making it a valuable ingredient in various products designed to kill or inhibit the growth of microorganisms. Additionally, CHLOROACETYL-GLYCYL-GLYCINE is used in cosmetic and personal care products for its antibacterial and preservative properties.

Check Digit Verification of cas no

The CAS Registry Mumber 15474-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,7 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15474-96:
(7*1)+(6*5)+(5*4)+(4*7)+(3*4)+(2*9)+(1*6)=121
121 % 10 = 1
So 15474-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H9ClN2O4/c7-1-4(10)8-2-5(11)9-3-6(12)13/h1-3H2,(H,8,10)(H,9,11)(H,12,13)

15474-96-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Chloroacetylglycylglycine

1.2 Other means of identification

Product number -
Other names 2-[[2-[(2-chloroacetyl)amino]acetyl]amino]acetic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15474-96-1 SDS

15474-96-1Relevant articles and documents

Conversion of Dipeptides and a Tetrapeptide to Macrocyclic Ionophores by means of Caesium Aided Ring Closure of the N-2-Chloroacetyl Derivatives

Kruizinga, Wim H.,Kingma, Rob,Leegstra, Libbe,Rokaszewski, Edward,Gruppen, Gert,Kellogg, Richard M.

, p. 1647 - 1648 (2007/10/02)

Three di-, (Gly)2, (Val)2 and (Leu)2, and one tetrapeptide, (Gly)4, have been acylated with 2-chloroacetyl chloride and the resulting products treated with Cs2CO3 in the dimethylformamide (DMF) solution; (Gly)2 and (Leu)2 provided strained 9-membered rings whereas (Val)2 dimerized to the 18-membered ring.

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